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BENZPHETAMINE HYDROCHLORIDE - 10702-040-10 - (benzphetamine hydrochloride)

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Drug Information of BENZPHETAMINE HYDROCHLORIDE

Product NDC: 10702-040
Proprietary Name: BENZPHETAMINE HYDROCHLORIDE
Non Proprietary Name: benzphetamine hydrochloride
Active Ingredient(s): 50    mg/1 & nbsp;   benzphetamine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of BENZPHETAMINE HYDROCHLORIDE

Product NDC: 10702-040
Labeler Name: KVK-TECH, INC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090968
Marketing Category: ANDA
Start Marketing Date: 20100721

Package Information of BENZPHETAMINE HYDROCHLORIDE

Package NDC: 10702-040-10
Package Description: 1000 TABLET in 1 BOTTLE (10702-040-10)

NDC Information of BENZPHETAMINE HYDROCHLORIDE

NDC Code 10702-040-10
Proprietary Name BENZPHETAMINE HYDROCHLORIDE
Package Description 1000 TABLET in 1 BOTTLE (10702-040-10)
Product NDC 10702-040
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name benzphetamine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100721
Marketing Category Name ANDA
Labeler Name KVK-TECH, INC
Substance Name BENZPHETAMINE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC]

Complete Information of BENZPHETAMINE HYDROCHLORIDE


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